Data / Medical devices / Specimen/Tissue, Identification Orientation / United States
FDA-registered makers of Specimen/Tissue, Identification Orientation in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Specimen/Tissue, Identification Orientation (product code MJI). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Specimen/Tissue, Identification Orientation
- Product code
- MJI
- Country
- United States
Makers of Specimen/Tissue, Identification Orientation in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Beekley Corporation | Bristol, CT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cancer Diagnostics, Inc. | Durham, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Evco Plastics, Div. Don Evans, Inc. | Deforest, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kite Endoscopic Innovations LLC | Concord Township, OH, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Leavitt Medical, Inc. | Lehi, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sanderson-Macleod, Inc. | Palmer, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sterilab, Inc. | Naples, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Taurus Engineering And Manufacturing, Inc. | Saint Paul, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tanis, Inc. | Delafield, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vector Surgical, LLC | Menomonee Falls, WI, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.